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由欧洲经济共同体赞助的关于检测诱变效应测试系统比较的协调研究工作综述

A review of the coordinated research effort on the comparison of test systems for the detection of mutagenic effects, sponsored by the E.E.C.

作者信息

Adler I D

出版信息

Mutat Res. 1980 Apr;74(2):77-93. doi: 10.1016/0165-1161(80)90234-4.

Abstract

Under the Environmental Research Programme of the Commission of the European Communities a coordinated comparative test programme was started to assess the mutagenic effects of chemicals in as many different assay systems as possible. A preliminary report is given on the results for 5 compounds selected by the Contact Group "Genetic Effects of Chemicals". 11 laboratories contributed data from tests in their expertise. The compounds were methyl methanesulfonate (MMS), N-nitrosodiethylamine (DEN), mitomycin C (MC), procarbazine (Natulan) and atrazine. The results of testing these 5 compounds in more than 20 test systems are still incomplete but some observations can be made at this time. MMS has been shown to be mutagenic in every system used in this collaborative effort which is not surprising in view of the fact that MMS is a widely used reference mutagen that does not require metabolic activation. Among the indirect mutagens which were tested, MC has been shown to be mutagenic with almost every system which has been applied. DEN which requires microsomal activation gave positive results in most submammalian systems as well as in mammalian cells in culture when the S9 fraction of liver homogenate was added. However, in whole mammals most results were negative. One study suggests that the difference in the results with DEN may be due to the short biological half-life of the mutagenically active metabolite. Procarbazine was negative in the microbial tests but gave a positive response in mammalian cells in culture, in Drosophila and in mammals. Atrazine has only been subjected to a limited amount of testing but the results indicate that plant metabolic activation is required in vitro, and that activation to a mutagenic metabolite also occurs in mammals independent from liver enzymes.

摘要

在欧洲共同体委员会的环境研究计划下,启动了一项协调的比较测试计划,以尽可能多的不同检测系统评估化学物质的致突变作用。本文给出了由“化学物质遗传效应”联络小组挑选的5种化合物的初步测试结果报告。11个实验室提供了各自专业领域的测试数据。这些化合物分别是甲磺酸甲酯(MMS)、N-亚硝基二乙胺(DEN)、丝裂霉素C(MC)、丙卡巴肼(纳治兰)和莠去津。在20多个测试系统中对这5种化合物进行测试的结果仍不完整,但目前可以得出一些观察结论。鉴于MMS是一种广泛使用的无需代谢激活的参考诱变剂,在本次合作研究中使用的每个系统中,MMS都显示出致突变性,这并不奇怪。在测试的间接诱变剂中,MC在几乎所有应用的系统中都显示出致突变性。需要微粒体激活的DEN,在添加肝脏匀浆的S9组分时,在大多数非哺乳动物系统以及培养的哺乳动物细胞中都给出了阳性结果。然而,在完整的哺乳动物中,大多数结果为阴性。一项研究表明,DEN结果存在差异可能是由于诱变活性代谢物的生物半衰期较短。丙卡巴肼在微生物测试中为阴性,但在培养的哺乳动物细胞、果蝇和哺乳动物中给出了阳性反应。莠去津仅接受了有限数量的测试,但结果表明,体外需要植物代谢激活,并且在哺乳动物中也会发生诱变代谢物的激活,且与肝脏酶无关。

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